Journal
FOOD CHEMISTRY
Volume 239, Issue -, Pages 984-992Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.foodchem.2017.07.029
Keywords
Gliadin; Thermal; Polymerization; Conformation; Viscoelasticity
Funding
- Natural Science Foundation of Jiangsu Province [BK20170708]
- National Natural Science Foundation of China [31471584]
- A Special Fund for Talents' Introduction Program of Jiangsu Superiority Disciplines [08080900238]
- Key Technology Research and Development Program of Jiangsu Province [BE2016360]
- Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions
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The physicochemical properties of gliadin upon mild thermal treatment were studied in terms of polymerization behavior, conformation and viscoelasticity. Gliadin samples were heated at 40, 60 and 90 degrees C for up to 20 min. Results showed that alpha-gliadin started to polymerize via disulfide (SS) bonds before gamma-gliadin at 90 degrees C, resulting in the extractability loss in aqueous ethanol. beta-Turn and specific beta-sheet structures were partially conversed to alpha-helices during thermal treatment. Rearrangement of noncovalent forces might contribute to viscosity loss of gliadin at 40 and 60 degrees C. However, the elevated elasticity at 90 degrees C was mainly due to gliadin polymerization while the viscosity variation was resulted from combined effects of non-covalent forces and covalent SS bonds. This study could offer insight into the variation of gliadin characteristics during the early baking process. (C) 2017 Elsevier Ltd. All rights reserved.
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